| HOME | HELP | FEEDBACK | SUBSCRIPTIONS | ARCHIVE | SEARCH | TABLE OF CONTENTS |
ARTICLES |
INSERM U-469, Centre CNRS-INSERM de Pharmacologie-Endocrinologie, 34094 Montpellier Cedex 5, France; and the Department of Anatomy and Neurobiology, University of Vermont College of Medicine (J.F.), Burlington, Vermont 05405
Address all correspondence and requests for reprints to: Dr. Patrice Mollard, INSERM U-469, Centre CNRS-INSERM de Pharmacologie-Endocrinologie, 141 rue de la Cardonille, 34094 Montpellier Cedex 5, France. E-mail: mollard{at}u469.montp.inserm.fr
Endocrine cells isolated from the anterior pituitary fire intracellular Ca2+ ([Ca2+]i) transients due to voltage-gated Ca2+ entry. However, the patterns of [Ca2+]i transients within the glandular parenchyma of the anterior pituitary are unknown. Here we describe, using real-time confocal laser microscopy, several spontaneous patterns of calcium signaling in acute pituitary slices prepared from male as well as cycling and lactating female rats. Forty percent of the cells demonstrated a spontaneous bursting mode, consisting of an active period of [Ca2+]i transients firing at a constant frequency, followed by a rest period during which cells were either silent or randomly active. The remaining recordings from endocrine cells either demonstrated random [Ca2+]i transients or were silent. These rhythmic bursts of [Ca2+]i transients, which required extracellular calcium, were detected in lactotrophs, somatotrophs, and corticotrophs within the acute slices. Of significance was the finding that the bursting mode could be adjusted by hypothalamic factors. In slices prepared from lactating rats, TRH recruited more bursting cells and finely adjusted the average duty cycle of [Ca2+]i bursts such that cells fired patterned bursts for approximately 70% of the recording period. Eighty-six percent of these cells were lactotrophs. Thus, the rhythmic [Ca2+]i bursts and their tuning by secretagogues may provide timing information that could encode for one or more cellular functions (e.g. exocytosis and/or gene expression) critical for the release of hormones by endocrine cells in the intact gland.
This article has been cited by other articles:
![]() |
I. M. Bur, A. M. Cohen-Solal, D. Carmignac, P.-Y. Abecassis, N. Chauvet, A. O. Martin, G. T. J. van der Horst, I. C. A. F. Robinson, P. Maurel, P. Mollard, et al. The Circadian Clock Components CRY1 and CRY2 Are Necessary to Sustain Sex Dimorphism in Mouse Liver Metabolism J. Biol. Chem., April 3, 2009; 284(14): 9066 - 9073. [Abstract] [Full Text] [PDF] |
||||
![]() |
A. Secondo, A. Pannaccione, M. Cataldi, R. Sirabella, L. Formisano, G. Di Renzo, and L. Annunziato Nitric oxide induces [Ca2+]i oscillations in pituitary GH3 cells: involvement of IDR and ERG K+ currents Am J Physiol Cell Physiol, January 1, 2006; 290(1): C233 - C243. [Abstract] [Full Text] [PDF] |
||||
![]() |
A. Ben-Shlomo, K. A. Wawrowsky, I. Proekt, N. M. Wolkenfeld, S.-G. Ren, J. Taylor, M. D. Culler, and S. Melmed Somatostatin Receptor Type 5 Modulates Somatostatin Receptor Type 2 Regulation of Adrenocorticotropin Secretion J. Biol. Chem., June 24, 2005; 280(25): 24011 - 24021. [Abstract] [Full Text] [PDF] |
||||
![]() |
G. N. Hyde, A. P. Seale, E. G. Grau, and R. J. Borski Cortisol rapidly suppresses intracellular calcium and voltage-gated calcium channel activity in prolactin cells of the tilapia (Oreochromis mossambicus) Am J Physiol Endocrinol Metab, April 1, 2004; 286(4): E626 - E633. [Abstract] [Full Text] [PDF] |
||||
![]() |
A. O. Martin, M.-N. Mathieu, and N. C. Guerineau Evidence for Long-Lasting Cholinergic Control of Gap Junctional Communication between Adrenal Chromaffin Cells J. Neurosci., May 1, 2003; 23(9): 3669 - 3678. [Abstract] [Full Text] [PDF] |
||||
![]() |
A. O. Martin, M.-N. Mathieu, C. Chevillard, and N. C. Guerineau Gap Junctions Mediate Electrical Signaling and Ensuing Cytosolic Ca2+ Increases between Chromaffin Cells in Adrenal Slices: A Role in Catecholamine Release J. Neurosci., August 1, 2001; 21(15): 5397 - 5405. [Abstract] [Full Text] [PDF] |
||||
![]() |
T. Fauquier, N. C. Guerineau, R. A. McKinney, K. Bauer, and P. Mollard Folliculostellate cell network: A route for long-distance communication in the anterior pituitary PNAS, June 28, 2001; (2001) 151339598. [Abstract] [Full Text] [PDF] |
||||
![]() |
C. Magoulas, L. McGuinness, N. Balthasar, D. F. Carmignac, A. K. Sesay, K. E. Mathers, H. Christian, L. Candeil, X. Bonnefont, P. Mollard, et al. A Secreted Fluorescent Reporter Targeted to Pituitary Growth Hormone Cells in Transgenic Mice Endocrinology, December 1, 2000; 141(12): 4681 - 4689. [Abstract] [Full Text] [PDF] |
||||
![]() |
F. Van Goor, D. Zivadinovic, A. J. Martinez-Fuentes, and S. S. Stojilkovic Dependence of Pituitary Hormone Secretion on the Pattern of Spontaneus Voltage-gated Calcium Influx. CELL TYPE-SPECIFIC ACTION POTENTIAL SECRETION COUPLING J. Biol. Chem., August 31, 2001; 276(36): 33840 - 33846. [Abstract] [Full Text] [PDF] |
||||
![]() |
T. Fauquier, N. C. Guerineau, R. A. McKinney, K. Bauer, and P. Mollard Folliculostellate cell network: A route for long-distance communication in the anterior pituitary PNAS, July 17, 2001; 98(15): 8891 - 8896. [Abstract] [Full Text] [PDF] |
||||
| HOME | HELP | FEEDBACK | SUBSCRIPTIONS | ARCHIVE | SEARCH | TABLE OF CONTENTS |
| Endocrinology | Endocrine Reviews | J. Clin. End. & Metab. |
| Molecular Endocrinology | Recent Prog. Horm. Res. | All Endocrine Journals |